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Form of workAbout the role
The Clinical Trial Coordinator manages the administration and conduct of Alzheimer’s Disease Clinical Trials. This is a Permanent Full Time position based in Malvern, Victoria.
Duties include:
- Managing key trial activities including recruitment, screening and on-study safety and efficacy visits.
- Practicing essential clinical documentation and data management processes according to Good Clinical Practice.
- Performing study specific procedures (ie. venepuncture, cognitive rating scales, ECGs).
- Conducting general administrative duties associated with Clinical Trial maintenance (ie. ensuring ISF is maintained; responding to queries).
About You
- At least 12 months prior experience in Clinical Trial research.
- Excellent understanding of GCP.
- Excellent record keeping skills with a keen eye for detail.
- Ability to work independently and as part of a team (including demonstrated organisational and problem-solving skills).
- Excellent communication skills, written and verbal.
- Strong administrative and computer skills.
Desirable
- Dementia Clinical Trial experience.
- Cognitive rating scale experience (including CDR, ADAS-Cog, MMSE, NPI etc.)
- Venepuncture, cannulation and ECG experience.
- GCP certification.
Ready to make a change? Apply Now by completing the application and attaching your CV & Cover letter!
All short-listed applicants for these positions will be asked to consent to a criminal record check.
